A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994254



Internal ID21903597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86416942..86418094hg38UCSC Ensembl
chr3:86466092..86467244hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994254
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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